Evidence map›Paper›PMID 32267835›Full record

ArticlePLoS biology2020

YTHDF2 promotes mitotic entry and is regulated by cell cycle mediators.

Qili Fei, Zhongyu Zou, Ian A Roundtree, Hui-Lung Sun, Chuan He

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
7.1field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

51 citing papers in PubMed, 111 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Targeting intracellular mRNA mJournal of advanced research · 2026
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. VIRMA-mediated mScience advances · 2025
    Article
  13. mAutism research : official journal of the International Society for Autism Research · 2025
    Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. RNA m6A methylation regulators in sepsis.Molecular and cellular biochemistry · 2024
    Review
  19. Differentiation and Growth-Arrest-Related lncRNA (International journal of molecular sciences · 2024
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 2 countries.

Qili FeiDepartment of Chemistry, The University of Chicago, Chicago, Illinois, United States of America.ORCID 0000-0002-0860-2175
Zhongyu ZouDepartment of Chemistry, The University of Chicago, Chicago, Illinois, United States of America.
Ian A RoundtreeDepartment of Chemistry, The University of Chicago, Chicago, Illinois, United States of America.
Hui-Lung SunDepartment of Chemistry, The University of Chicago, Chicago, Illinois, United States of America.ORCID 0000-0003-2273-311X
Chuan HeDepartment of Chemistry, The University of Chicago, Chicago, Illinois, United States of America.
Howard Hughes Medical Institute · US

Funding

Transcriptome-wide base-resolution sequencing of pseudouridine in human normal and AD brain tissues-CEGS Admin supplement 2020-2021RM1HG008935 · NHGRI · UNIVERSITY OF CHICAGO · PI HE, CHUAN · 2016 to 2025
$24.4M
Recognition and mechanism of N6-methyl adenosine modificationsR01GM113194 · NIGMS · UNIVERSITY OF CHICAGO · PI PAN, TAO · 2015 to 2022
$2.5M
NHGRI NIH HHS RM1 HG008935NIGMS NIH HHS R01 GM113194
6 · The paper itself

Abstract

The N6-methyladenosine (m6A) modification regulates mRNA stability and translation. Here, we show that transcriptomic m6A modification can be dynamic and the m6A reader protein YTH N6-methyladenosine RNA binding protein 2 (YTHDF2) promotes mRNA decay during cell cycle. Depletion of YTHDF2 in HeLa cells leads to the delay of mitotic entry due to overaccumulation of negative regulators of cell cycle such as Wee1-like protein kinase (WEE1). We demonstrate that WEE1 transcripts contain m6A modification, which promotes their decay through YTHDF2. Moreover, we found that YTHDF2 protein stability is dependent on cyclin-dependent kinase 1 (CDK1) activity. Thus, CDK1, YTHDF2, and WEE1 form a feedforward regulatory loop to promote mitotic entry. We further identified Cullin 1 (CUL1), Cullin 4A (CUL4A), damaged DNA-binding protein 1 (DDB1), and S-phase kinase-associated protein 2 (SKP2) as components of E3 ubiquitin ligase complexes that mediate YTHDF2 proteolysis. Our study provides insights into how cell cycle mediators modulate transcriptomic m6A modification, which in turn regulates the cell cycle.

Indexed as

AdenosineCDC2 Protein KinaseCell CycleCell Cycle ProteinsCullin ProteinsDNA-Binding ProteinsHeLa CellsHumansMitosisProtein StabilityProtein-Tyrosine KinasesRNA-Binding ProteinsRNA StabilityS-Phase Kinase-Associated ProteinsAdenosineCDC2 Protein KinaseCDK1 protein, humanCell Cycle ProteinsCullin 1Cullin ProteinsDDB1 protein, humanDNA-Binding ProteinsN-methyladenosineProtein-Tyrosine KinasesRNA-Binding ProteinsSKP2 protein, humanS-Phase Kinase-Associated ProteinsWEE1 protein, humanYTHDF2 protein, human

Identifiers

PMID32267835
PMCPMC7170294
OpenAlexW3014546597

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.